Diagnostic Method

ABSTRACT

The present invention concerns a method for the detection or monitoring of cancer using a biological sample selected from blood, plasma, serum, saliva, urine from an individual, said method comprising: (a) obtaining DNA from the said biological sample; (b) digesting the DNA sample with one or more methylation-sensitive restriction enzymes; (c) quantifying or detecting a DNA sequence of interest after step (b), wherein the target sequence of interest contains at least two methylation-sensitive restriction enzyme recognition sites; and (d) comparing the level of the DNA sequence from the individual to a normal standard, to detect, prognosticate or monitor cancer.

CROSS REFERENCE TO RELATED PATENT APPLICATION

This application claims the benefit of the filing date of U.S. provisional patent application 60/847,499, filed Sep. 27, 2006, the disclosure of which is herein incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to methods for diagnosis, prognosis or monitoring of cancer in an individual, in particular using the differential methylation patterns in genes associated with cancers.

BACKGROUND TO THE INVENTION

It is well known that many tumor suppressor genes are methylated in tumor cells. As such, the use of methylation markers has been suggested for the detection or monitoring of cancer in patients. A number of different methods have been proposed for detection of these methylated sequences.

Methylation specific PCR (MSP) is the most commonly used method for detecting methylated or unmethylated DNA. MSP involves the step of bisulfite conversion. Sodium bisulfite is used to deaminate cytosine to uracil while leaving 5-methyl-cytosine intact. Methylation-specific PCR uses PCR primers targeting the bisulfite induced sequence changes to specifically amplify either methylated or unmethylated alleles. Bisulfite conversion destroys about 95% of the DNA. Since DNA concentrations are typically very low in the serum or plasma, a 95% reduction in DNA results in a detection rate of less than 50%.

Alternative methods use restriction enzymes that digest specifically either the methylated or unmethylated DNA. Enzymes that cut specifically methylated DNA are rare. However, enzymes that cut specifically unmethylated DNA are more readily available. Detection methods then establish whether digestion has occurred or not, and thus depending on the specificity of the enzyme used, allows detection of whether the underlying DNA was methylated or unmethylated and thus associated with cancer or not.

Methylation-sensitive enzyme digestion has been previously proposed. For example, Silva et al, British Journal of Cancer, 80:1262-1264, 1999 conducted methylation-sensitive enzyme digestion followed by PCR. However, as noted by the authors Yegnasubramanian et al, Nucleic Acids Research, Vol. 34, No. 3, 2006 e19, such methods are plagued by the number of false-positives that are generated.

The present invention seeks to provide enhanced methods of methylation-sensitive detection which eliminate or reduce false positives and/or false negatives.

SUMMARY OF THE INVENTION

In accordance with the present invention, there is provided a method for the detection or monitoring of cancer using a biological sample selected from blood, plasma, serum, saliva, urine from an individual, said method comprising:

-   -   (a) obtaining DNA from the said biological sample;     -   (b) digesting the DNA sample with one or more         methylation-sensitive restriction enzymes;     -   (c) quantifying or detecting a DNA sequence of interest after         step (b), wherein the target sequence of interest contains at         least two methylation-sensitive restriction enzyme recognition         sites; and     -   (d) comparing the level of the DNA sequence from the individual         to a normal standard, to detect, prognosticate or monitor         cancer.

In a preferred aspect of the present invention, the polymerase chain reaction is used in step (c). Preferably, the methylation-sensitive restriction enzyme recognises DNA sequences which have not been methylated. The target sequence is a sequence susceptible to methylation in cancer patients so that an unmethylated target sequence in a normal patient is digested and is not amplified by the polymerase chain reaction, whereas in a cancer patient, the target sequence is methylated and is not digested by the enzyme and can subsequently be quantified or detected, for example using the polymerase chain reaction.

The methods of the present invention can be used to predict the susceptibility to cancer of the individual, to assess the stage of cancer in the individual, to predict the likelihood of overall survival for the individual, to predict the likelihood of recurrence for the individual or to assess the effectiveness of treatment in the individual.

In accordance with another aspect of the present invention, there is provided a method for the detection or monitoring of cancer using a biological sample selected from blood, plasma, serum, saliva, urine from an individual, said method comprising:

(a) obtaining DNA from the said biological sample;

(b) digesting the DNA sample with one or more methylation-sensitive restriction enzymes;

(c) quantifying or detecting a DNA sequence of interest after step (b) wherein the DNA sequence is a sequence comprising part or all of RASSF1A; and

(d) comparing the level of the DNA sequence from the individual to a normal standard, to detect, prognosticate or monitor cancer.

In accordance with a further aspect of the invention, there is provided probes, primers and kits for use in the method of the invention. In particular, there is provided:

-   -   a detectably-labelled probe for the detection or monitoring of         cancer in a biological sample selected from blood, plasma,         serum, saliva, urine from an individual, which comprises the         sequence shown it SEQ ID NO: 4;     -   a set of primers for the detection or monitoring of cancer in a         biological sample selected from blood, plasma, serum, saliva,         urine from an individual, which comprises a primer comprising         the sequence shown in SEQ ID NO: 2 and a primer comprising the         sequence shown in SEQ ID NO: 3;     -   a kit for the detection or monitoring of cancer in a biological         sample selected from blood, plasma, serum, saliva, urine from an         individual, which comprises the probe of the invention and the         set of primers of the invention     -   a detectably-labelled probe for use as a control during the         detection or monitoring of cancer in a biological sample         selected from blood, plasma, serum, saliva, urine from an         individual, which comprises the sequence shown in SEQ ID NO: 7;     -   a set of primers for use as a control during the detection or         monitoring of cancer in a biological sample selected from blood,         plasma, serum, saliva, urine from an individual, which comprises         a primer comprising the sequence shown in SEQ ID NO: 5 and a         primer comprising the sequence shown in SEQ ID NO: 6; and     -   a kit for use as a control during the detection or monitoring of         cancer in a biological sample selected from blood, plasma,         serum, saliva, urine from an individual, which comprises the         control probe of the invention and the set of control primers of         the invention.

DESCRIPTION OF THE FIGURES

FIG. 1: concentration of methylated RASSF1A in patients' plasma.

FIG. 2: changes of plasma methylated RASSF1A levels after surgical resection of hepatocellular carcinoma (HCC).

FIG. 3: methylated RASSF1A sequence concentration in plasma prior to surgical resection is predictive of patient survival after surgical resection.

FIG. 4: methylated RASSF1A sequence concentration in plasma post-surgical resection is predictive of patients survival after surgical resection.

FIG. 5: concentration of methylated RASSF1A detected in the plasma of nasopharangeal carcinoma (NPC) patients correlated with Epstein-Barr virus (EBV) DNA concentration.

FIG. 6: Genomic sequence of the promoter and the first exon of the RASSF1A gene (SEQ ID NO: 1). The recognition sequence of the methylation-sensitive restriction enzyme BstUI is underlined and the target sequence for PCR detection is highlighted in bold. There are 5 BstUI enzyme restriction sites in the target sequence.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a method to assess, diagnose, prognosticate or monitor the presence or progression of tumors in an individual. The method involves the use of a methylation-sensitive restriction enzyme to digest DNA sequences. DNA sequences of interest are selected which contain at least two restriction sites which may or may not be methylated. The method is preferably carried out with methylation-sensitive restriction enzymes which preferentially cleave unmethylated sequences compared to methylated sequences. Methylated sequences remain undigested and are detected. Digestion of unmethylated sequences at least one of the methylation-sensitive restriction enzyme sites results in the target sequence not being detected or amplifiable. Thus a methylated sequence can be distinguished from an unmethylated sequence. In one embodiment of the invention, the quantity of uncut target sequence detected in a biological sample, e.g. plasma or serum of cancer patients is higher than that demonstrated in a biological sample of the same type of healthy or cancer-free individuals since the target sequences are more highly methylated in cancer patients than healthy individuals.

In the alternative, restriction enzymes which cut methylated DNA can be used. Unmethylated DNA sequences are not digested and can be detected. In another embodiment of this invention, lower quantities of the uncut DNA sequence are detected in a biological sample, e.g. plasma or serum of cancer patients when compared with that demonstrated in a biological sample of the same type in cancer-free individuals.

In a preferred embodiment according to the present invention, the target sequence is detected by amplification by PCR. Real-time quantitative PCR can be used. Primer sequences are selected such that at least two methylation-sensitive restriction enzyme sites are present in the sequence to be amplified using such primers. The methods in accordance with the present invention do not use sodium bisulfite. Amplification by a suitable method, such as PCR, is used to detect uncut target sequence, and thus to identify the presence of methylated DNA which has not been cut by restriction enzymes.

In accordance with the present invention, any suitable methylation-sensitive restriction enzyme can be used. Examples of methylation-sensitive restriction enzymes that cut unmethylated DNA are listed in Table I below. TABLE I Examples of methylation-sensitive restriction enzymes: The letter codes in the recognition sequences represent different combinations of nucleotides and are summarised as follows: R = G or A; Y = C or T; W = A or T; M = A or C; K = G or T; S = C or G; H = A, C or T; V = A, C or G; B = C, G or T; D = A, G or T; N = G, A, T or C. The CpG dinucleotide(s) in each recognition sequence is/are underlined. The cytosine residues of these CpG dinucleotides are subjected to methyiation. Effect of CpG methylation Enzyme Recognition sequence on enzyme restriction* AatII GACGTC blocked AjiI CACGTC blocked BstUI, Bsh1236I CGCG blocked Bsh1285I CGRYCG blocked BshTI ACCGGT blocked Bsp68I TCGCGA blocked Bsp119I TTCGAA blocked Bsp143II RGCGCY blocked Bsu15I ATCGAT blocked CseI GACGC blocked Cfr10I RCCGGY blocked Cfr42I CCGCGG blocked CpoI CGGWCCG blocked Eco47III AGCGCT blocked Eco52I CGGCCG blocked Eco72I CACGTG blocked Eco105I TACGTA blocked EheI GGCGCC blocked Esp3I CGTCTC blocked FspAI RTGCGCAY blocked HhaI; Hin6I GCGC blocked Hin1I GRCGYC blocked HpaII CCGG blocked Kpn2I TCCGGA blocked MluI ACGCGT blocked NotI GCGGCCGC blocked NsbI TGCGCA blocked PauI GCGCGC blocked PdiI GCCGGC blocked Pfl123II CGTACG blocked Ppu21I YACGTR blocked Psp1406I AACGTT blocked PvuI CGATCG blocked SalI GTCGAC blocked SgsI GGCGCGCC blocked SmaI CCCGGG blocked SmuI CCCGC blocked SsiI CCGC blocked TaiI ACGT blocked TauI GCSGC blocked *The methylation of the cytosine of the CpG dinucleotides in the recognition sequence would prevent enzyme cutting of the target sequence.

The target sequence includes two or more methylation-sensitive restriction enzyme sites. Such sites may be recognised by the same or different enzymes. However, the sites are selected so that at least two sites in each sequence are digested when unmethylated when using enzymes which preferentially cleave unmethylated sequences compared to methylated sequences.

In a less preferred embodiment the target sequence contains at least two sites which are cut or cleaved by restriction enzymes which preferentially cleave methylated sequences. The two or more sites may be cleaved by the same or different enzymes.

Any suitable DNA methylation marker may be used in accordance with the present invention. Such DNA methylation markers are those where the selected sequence shows a different methylation pattern in cancer patients compared to normal individuals. Suitable markers are selected such that the sequence to be amplified contains at least two methylation-sensitive restriction enzyme sites. Generally such methylation markers are genes where promoter and/or encoding sequences are methylated in cancer patients. Preferably the selected sequences are not methylated or are methylated to a lesser extent in non-cancer or cancer-free individuals.

Suitable DNA methylation markers include, for example, RASSF1A. Indeed, RASSF1A has proved to be particularly effective for use in detection or monitoring of cancer in an individual. Thus, in accordance with an alternative aspect of the present invention, there is provided a method for the detection or monitoring of cancer using a biological sample selected from blood, plasma, serum, saliva, urine from an individual, said method comprising:

(a) obtaining DNA from the said biological sample;

(b) digesting the DNA sample with one or more methylation-sensitive restriction enzymes;

(c) quantifying or detecting a DNA sequence of interest after step (b) wherein the DNA sequence is a sequence comprising part or all of RASSF1A; and

(d) comparing the level of the DNA sequence from the individual to a normal standard, to detect, prognosticate or monitor cancer.

The tumor types associated with RASSF1A promoter hypermethylation are listed in Table II below. TABLE II Frequencies of RASSF1A promoter hypermethylation in different types of cancers (ordered in descending frequency): Frequencies of RASSF1A promoter Cancer types hypermethylation References Liver  93%-100% (1-4) Breast 49%-95% (5-8) Lung (small cell) 79%-88% (9, 10) Prostate 71%-83% (11-13) Melanoma 41%-75% (14, 15) Pancreas 64% (16) Kidney 36%-64% (17-19) Bladder 47%-60% (20, 21) Colon 12%-45% (19, 22-24) Ovary 30%-40% (19, 25, 26) Lung (non-small cell) 28%-40% (9, 27, 28) References for Table II

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Other preferred tumor suppressor genes showing hypermethylation in tumors are listed in Table III. TABLE III Examples of tumor suppressor genes which promoter regions are frequently inactivated by methylation in cancers: Tumor Types of cancer in which the suppressor gene may be aberrantly gene methylated References APC colorectal, breast, head and (1-13) neck, esophagus, bladder, prostate, stomach, lung, kidney DAP-kinase pancreas, stomach, lung, (9, 10, 14-19) colorectal, breast, cervix, nasopharynx E-cadherin breast, lung, stomach, (8, 20-27) colorectal, prostate, bladder, cervix, kidney GSTPI lung, stomach, bladder, (8, 9, 11, 12, 28-31) prostate, breast, cervix hMLH1 stomach, colorectal, cervix, (6, 9, 16, 21, 31-34) liver, esophagus, lung, ovary, prostate MGMT lung, colorectal, bladder (8, 11, 13, 15-17, 28, cervix, breast, esophagus, 31, 35, 36) prostate, nasopharynx, kidney NORE1A kidney, lung, breast, colon (37-39) p14 colorectal, bladder, (11, 13, 16, 19, 40-42) nasopharynx, kidney, stomach, breast p15 bladder, nasopharynx, kidney, (7, 11, 19, 27, 43-46) multiple myeloma, colorectal, lung, ovary, stomach P16INK4a lung, stomach, bladder, cervix, (8, 9, 11, 15, 17, 18, nasopharynx, breast, prostate, 27, 28, 35, 43, 44, 47- kidney, liver, colorectal, 49) pancreas, leukemia, multiple myeloma, thyroid RARbeta lung, breast, nasopharynx, (8, 12, 13, 19, 23, 30, prostate, kidney, stomach 35, 50) SOCS1 colorectal, leukemia, stomach, (51-57) ovary, liver, pancreas Rb retinoblastoma, lung, (58-61) esophagus, stomach VHL kidney (13, 62) References for Table III:

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Cancer Res 2006; 66:2000-11.

In accordance with the method of the present invention a sample is taken or obtained from the patient. Suitable samples include blood, plasma, serum, saliva and urine. Samples to be used in accordance with the present invention include whole blood, plasma or serum. Methods for preparing serum or plasma from whole blood are well known among those of skill in the art. For example, blood can be placed in a tube containing EDTA or a specialised commercial product such as Vacutainer SST (Becton Dickenson, Franklin Lake, N.J.) to prevent blood clotting, and plasma can then be obtained from whole blood through centrifugation. Serum may be obtained with or without centrifugation following blood clotting. If centrifugation is used then it is typically, though not exclusively conducted at an appropriate speed, for example, 1500-3000×g Plasma or serum may be subjected to additional centrifugation steps before being transferred to a fresh tube for DNA extraction.

Preferably, DNA is extracted from the sample using a suitable DNA extraction technique. Extraction of DNA is a matter of routine for one of skill in the art. There are numerous known methods for extracting DNA from a biological sample including blood. General methods of DNA preparation, for example described by Sambrook and to Russell, Molecular Cloning a Laboratory Manual, 3^(rd) Edition (2001) can be followed. Various commercially available reagents or kits may also be used to obtain DNA from a blood sample.

In accordance with the invention, the DNA containing sample is incubated with one or more restriction enzyme(s) which preferentially cut unmethylated DNA under conditions such that where two or more restriction enzyme sites are present in the target sequence in the unmethylated state, the restriction enzyme(s) can cut the target sequence at least one such site. In accordance with an alternative aspect of the invention, a DNA sample is incubated with one or more restriction enzymes which only cut methylated DNA under conditions such that where two or more restriction enzyme sites are present in the methylated state, the restriction enzyme(s) can cut the target sequence at least one such site.

Preferably samples are incubated under conditions to allow complete digestion. This may be achieved, for example by increasing the incubation times and/or increasing the quantity of the enzyme used. Typically, the sample will be incubated with 100 active units of methylation-sensitive restriction enzyme for a period of up to 16 hours. It is a matter of routine for one of skill in the art to establish suitable conditions based on the quantity of enzyme used.

After incubation, uncut target sequences are detected. Preferably, these sequences are detected by amplification, for example using the polymerase chain reaction (PCR).

DNA primers are designed to amplify a sequence containing at least two methylation-sensitive restriction enzyme sites. Such sequences can be identified by looking at DNA methylation markers and identifying restriction enzyme sites within those markets which are recognised by methylation-sensitive enzymes. For example using the recognition sequences for the methylation-sensitive enzymes identified in Table I, suitable target sequences can be identified in the methylation markers listed in Table III.

Using RASSF1A as an example, the target sequence may comprise part or all of the promoter sequence and/or exon 1 of the RASSF1A gene. The sequence for the promoter and axon 1 is set out in FIG. 6 (SEQ ID NO: 1). In a preferred embodiment the target sequence for detection is that highlighted in bold in FIG. 6 (residues 1142 to 1269 of SEQ ID NO: 1). In a more preferred embodiment residues 1142 to 1269 of SEQ ID NO: 1 are amplified using (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 2 and (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 3. In another more preferred embodiment residues 1142 to 1269 of SEQ ID NO: 1 are detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 4. In an even more preferred embodiment residues 1142 to 1269 of SEQ ID NO: 1 are detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 4 and no additional nucleotides.

When using methylation-sensitive enzymes, altered quantities of the target sequence will be detected depending on the methylation status of the target sequence in a particular individual. In the preferred aspect of the present invention using methylation-sensitive restriction enzymes which preferentially cut unmethylated DNA, the target sequence will not be detected in the unmethylated state, for example in a healthy individual. However, where the target sequence is methylated, for example in a selected sample from a cancer patient, the target sequence is not cut by the restriction enzyme and the target sequence can thus be detected by PCR.

Thus, the method can be used to determine the methylation status of the target sequence and provide an indication of the cancer status of the individual.

The methods of the present invention may additionally include quantifying or detecting a control sequence. The control sequence is selected which does not show aberrant methylation patterns in cancer. In accordance with a preferred aspect of the present invention, the control sequence is selected to contain at least two methylation-sensitive restriction enzyme recognition sites. Preferably, the control sequence is selected to contain the same number of methylation-sensitive restriction enzyme recognition sites as the DNA sequence of interest. Typically the presence or absence of such control sequences is detected by amplification by the polymerase chain reaction after digestion with the methylation-sensitive restriction enzyme(s). Such control sequences can be used to assess the extent of digestion with the one or more methylation-sensitive restriction enzymes. For example, if after digestion with the methylation-sensitive restriction enzyme(s) control sequences are detectable, this would indicate that the digestion is not complete and the methods can be repeated to ensure that complete digestion has occurred. Preferably the control sequence is selected to contain the same methylation-sensitive restriction enzyme sites that are present in the target sequence. In a preferred embodiment the control sequence is β-actin. In a more preferred embodiment a target sequence in the β-actin is amplified using (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 5 and (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 6. In an even more preferred embodiment the target sequence in β-actin (which is amplified using primers comprising SEQ ID NOs: 5 and 6) is detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 7. In an even more preferred embodiment the target sequence is detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 7 and no additional nucleotides.

The present methods can be used to assess the tumor status of an individual. The methods can be used, for example, in the diagnosis and/or prognosis of cancer. The methods can also be used to monitor the progress of cancer, for example, during treatment. The methods can also be used to monitor changes in the levels of methylation over time, for example to assess the susceptibility of an individual to cancer, and the progression of the disease. The methods can also be used to predict the outcome of disease or the likelihood of success of treatment.

In a preferred aspect of the present invention the target sequence is RASSF1A and is used in the diagnosis of cancer. For example, RASSF1A methylation can be used to detect and monitor hepatocellular or nasopharyngeal carcinoma. The method is particularly useful in monitoring the susceptibility of a hepatitis B carrier or a hepatitis C carrier to hepatocellular carcinoma.

In another aspect of the invention, there is provided probes and primers for use in the method of the invention. Firstly, there is provided a set of primers or a detectably-labelled probe for the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual. The set of primers comprises or consists of (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 2 and (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 3. The set of primers is capable of amplifying residues 1142 to 1269 of SEQ ID NO: 1 (i.e. part of the promoter and first exon of the RASSF1A gene). The detectably-labelled probe comprises the sequence shown in SEQ ID NO: 4 and is capable of detecting residues 1142 to 1269 of SEQ ID NO: 1. The detectably-labelled probe preferably comprises the sequence shown in SEQ ID NO: 4 and no additional nucleotides. The detectably-labelled probe is most preferably the probe used in the Examples.

Secondly, there is provided a set of primers and a detectably-labelled probe for use as a control during the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual. The set of primers comprises or consists of (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 5 and (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 6. The set of primers is capable of amplifying a target sequence in β-actin. The detectably-labelled probe comprises the sequence shown in SEQ ID NO: 7 and is capable of detecting the target sequence in β-actin that is amplified by the primers comprising SEQ ID NOs: 5 and 6. The detectably-labelled probe preferably comprises the sequence shown in SEQ ID NO: 7 and no additional nucleotides. The detectably-labelled control probe is most preferably the control probe used in the Examples.

The probes are detectably-labelled. The detectable label allows the presence or absence of the hybridization product formed by specific hybridization between the probe and the target sequence to be determined. Any label can be used. Suitable labels include, but are not limited to, fluorescent molecules, radioisotopes, e.g. ¹²⁵I, ³⁵S, enzymes, antibodies and linkers such as biotin.

In another aspect, there is provided kits for use in the method of invention. Firstly, there is provided a kit for the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual. The kit comprises (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 2, (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 3 and (c) a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 4 and optionally no additional nucleotides. The kit is capable of amplifying and detecting residues 1142 to 1269 of SEQ ID NO: 1.

Secondly, there is provided a kit for use as a control during the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual. The kit comprises (a) a primer comprising or consisting of the sequence shown in SEQ ID NO: 5, (b) a primer comprising or consisting of the sequence shown in SEQ ID NO: 6 and (c) a detectably-labelled probe comprising the sequence shown in SEQ ID NO: 7 and optionally no additional nucleotides. The kit is capable of amplifying and detecting a target sequence in β-actin.

The kits of the invention may additionally comprise one or more other reagents or instruments which enable the method of the invention as described above to be carried out. Such reagents or instruments include one or more of the following: suitable buffer(s) (aqueous solutions), PCR reagents, fluorescent makers and/or reagents, means to obtain a sample from individual subject (such as a vessel or an instrument comprising a needle) or a support comprising wells on which reactions can be done. Reagents may be present in the kit in a dry state such that the fluid sample resuspends the reagents. The kit may, optionally, comprise instructions to enable the kit to be used in the method of the invention.

The invention is hereinafter described in more detail by reference to the Examples below.

EXAMPLES

Sixty-three hepatocellular carcinoma (HCC) patients, as well as two groups of controls, were recruited. The first control group consisted of 15 healthy control subjects without chronic hepatitis B infection. The second control group consisted of chronic hepatitis B carriers. For each HCC patient, one sex- and age-matched chronic hepatitis B carrier was recruited as a control. Chronic hepatitis B carriers had increased risk of developing HCC and, thus, would be the target group for HCC screening. Four milliliters of venous blood were collected from each study subject into EDTA-containing tubes. Blood samples were centrifuged at 1,600 g for 10 min and the supernatant was re-centrifuged at 16,000 g for 10 min. DNA was then extracted from 800 μL of plasma using the QIAamp mini kit (Qiagen, Hilden, Germany) and eluted with 50 μL of H₂O. Thirty-five microliters of plasma DNA were digested with 100 U of BstU I enzyme, in 1× digestion buffer at 60° C. for 16 hours.

The concentration of plasma RASSF1A sequence was determined by real-time PCR using the primers 5′AGCCTGAGCTCATTGAGCTG3′ (SEQ ID NO: 2) and 5′ACCAGCTGCCGTGTGG3′ (SEQ ID NO: 3), and the probe 5′FAM-CCAACGCGCTGCGCAT(MGB)3′ (SEQ ID NO: 4). Each reaction contains 1× TaqMan Universal PCR Master Mix (Applied Biosystem, Foster City), 300 nM each of the primers and 85 nM of probes. 7.15 microliters of enzyme-digested plasma DNA mixture (equivalent to 5 μL of undigested plasma DNA) were used as the template for each PCR reaction. The thermal profile was 50° C. for 2 minutes, 95° C. for 10 minutes, 50 cycles of 95° C. for 15 seconds and 60° C. for 1 minute. All reactions were run in duplicate and the mean quantity was taken. The RASSF1A amplicon embraced 5 restriction sites of BstUI.

To ensure the completeness of the restriction enzyme digestion, real-time PCR targeting the β-actin gene was performed for each enzyme digested samples using the primers 5′GCGCCGTTCCGAAAGTT3′ (SEQ ID NO: 5) and 5′CGGCGGATCGGCAAA3′ (SEQ ID NO: 6), and the probe 5′FAM-ACCGCCGAGACCGCGTC(MGB)3′ (SEQ ID NO: 7). By bisulfite sequencing, the β-actin gene promoter was shown to be completely unmethylated in blood cells and HCC tissues. The β-actin amplicon is of similar size of the RASSF1A amplicon and contains identical number of BstUI enzyme restriction sites.

To investigate if the enzyme digestion efficiencies for unmethylated RASSF1A and β-actin sequences were similar, aliquots of 1 μg of buffy coat were digested with 100 U of BstU I enzyme for different time intervals (15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 120 minutes, 3 hours, 4 hours, 5 hours, 6 hours, 12 hours and 16 hours). The concentrations of RASSF1A and β-actin sequences were measured in each sample after the enzyme digestion. As shown in FIG. 1, the concentrations of RASSF1A and β-actin sequences in these buffy coat DNA showed a positive correlation (r=0.986, P<0.0001, Pearson correlation). As the enzyme digestion efficiencies for unmethylated RASSF1A and β-actin sequences are similar, the completeness of the digestion of unmethylated RASSF1A sequence should be reflected by the absence of β-actin sequence in the digested plasma DNA sample. Therefore, all samples with positive β-actin signal were subject to further enzyme digestion until no β-actin sequence was detectable in the digested plasma DNA sample.

After BstUI enzyme digestion, RASSF1A sequences were detected in the plasma of 59 (93%) of the 63 HCC patients and 37 (58%) of the 63 matched chronic hepatitis B carriers (HBV carriers). These results are shown in FIG. 2. The median plasma RASSF1A concentrations of the HCC patients and chronic hepatitis B carriers were 770 copies/mL and 118 copies/mL, respectively. In contrast, RASSF1A was not detectable in the plasma of any of the 15 healthy subjects.

FIG. 3 demonstrates that the survival probabilities of HCC patients with preoperative plasma RASSF1A concentration of less than 550 copies/mL were better than those with levels higher than 550 copies/mL (p=0.0359, Kaplan-Meier survival analysis).

Blood samples were collected from the HCC patients at 1 month after the surgical resection of the tumor. In the 59 patients with detectable plasma RASSF1A before tumor resection, 45 of them (76%) showed a reduction in the concentration after the operation. These results are shown in FIG. 4. Among these 45 patients, 13 of them had undetectable RASSF1A after the resection of tumor. The median RASSF1A concentration dropped from 770 copies/mL to 250 copies/mL (p<0.0001, Wilcoxon test).

To further investigate if the quantitative analysis of plasma RASSF1A after methylation-sensitive restriction enzyme digestion is a generic marker for cancers with aberrant methylation of RASSF1A, 67 nasopharyngeal carcinoma (NPC) patients were recruited for the study of the correlation of the plasma concentrations of enzyme-digestion-resistant RASSF1A and Epstein-Barr virus (EBV) DNA. Plasma EBV DNA is an established marker for NPC and has been shown to reflect tumor load (Lo Y M D, Chan L Y, Lo K W, Leung S F, Zhang J, Chan A T, Lee J C, Hjelm N M, Johnson P J, Huang D P. Quantitative analysis of cell-free Epstein-Barr virus DNA in plasma of patients with nasopharyngeal carcinoma. Cancer Res 1999; 59:1199-91). The results are shown in FIG. 5. EBV DNA and enzyme-digestion-resistant RASSF1A sequence were detectable in the plasma of 65 (940%) and 37 (54%) patients, respectively. In the patients with detectable enzyme-digestion-resistant RASSF1A and EBV DNA, the plasma concentrations of the two DNA sequences showed a positive correlation (r=0.343, p=0.037, Spearman correlation). 

1. A method for the detection or monitoring of cancer using a biological sample selected from blood, plasma, serum, saliva, urine from an individual, said method comprising: (a) obtaining DNA from the said biological sample; (b) digesting the DNA sample with one or more methylation-sensitive restriction enzymes; (c) quantify or detecting a DNA sequence of interest after step (b), wherein the target sequence of interest contains at least two methylation-sensitive restriction enzyme recognition sites; and (d) comparing the level of the DNA sequence from the individual to a normal standard, to detect prognosticate or monitor cancer.
 2. The method according to claim 1, wherein the polymerase chain reaction (PCR) is used in step (c), and the PCR amplicon contains at least two recognition sites for the methylation-sensitive restriction enzyme used in step (b).
 3. The method according to claim 1, wherein real-time quantitative polymerase chain reaction (Q-PCR) is used in step (c) and the PCR amplicon contains at least two recognition sites for the methylation-sensitive restriction enzyme used in step (b).
 4. The method according to claim 1, wherein the DNA sequence quantified in step (c) is a sequence comprising part or all of RASSF1A, or other tumor suppressor genes or other genes which demonstrate aberrant DNA methylation patterns in cancer.
 5. The method according to claim 4, wherein the DNA sequence is selected from the promoter, exon 1, or fragments thereof of RASSF1A.
 6. The method according to claim 5, wherein the DNA sequence is residues 1142 to 1269 of SEQ ID NO:
 1. 7. The method according to claim 6, wherein: (a) the DNA sequence is amplified using a primer comprising the sequence shown in SEQ ID NO: 2 and a primer comprising the sequence shown in SEQ ID NO: 3; and/or (b) the DNA sequence is detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO:
 4. 8. The method according to claim 1, wherein following the enzymatic treatment step (b), each target DNA molecule of the sequence of interest in the sample is cut at least one methylation-sensitive restriction enzyme site by the methylation-sensitive restriction enzyme(s) when present in the unmethylated state.
 9. The method according to claim 1, wherein in step (b) the sample is treated with an excess of the enzyme(s), and/or wherein the incubation time is extended.
 10. The method according to claim 1, wherein the level of the DNA sequence quantified after the enzymatic treatment is used to: (a) diagnose cancer in the individual (b) predict the susceptibility to cancer of the individual; (c) assess the stage of the cancer in the individual; (d) predict the likelihood of overall survival for the individual; (e) predict the likelihood of recurrence for the individual; or (f) assess the treatment effectiveness for the individual.
 11. The method of claim 10, wherein the trend of the level of the DNA sequence after the enzymatic treatment over the time course of treatment, monitoring or post-treatment is quantified.
 12. The method according to claim 11, wherein the DNA sequence comprises part or all of RASSF1A and wherein the method is used in the diagnosis, prognosis or monitoring of hepatocellular carcinoma or nasopharyngeal carcinoma.
 13. The method according to claim 12, wherein the individual is a hepatitis carrier.
 14. The method according to claim 13, wherein the individual is a hepatitis B carrier or a hepatitis C carrier.
 15. The method according to claim 1, wherein the method further comprises quantifying or detecting a control DNA sequence in the DNA sample that has been digested with one or more methylation-sensitive restriction enzyme(s) wherein said control sequence does not demonstrate aberrant DNA methylation patterns in cancer.
 16. The method according to claim 15, wherein at least two methylation-sensitive restriction enzyme recognition sites are present in the control sequence.
 17. The method according to claim 16, wherein the same number of methylation-sensitive restriction enzyme recognition sites are present in the control sequence and the target sequence.
 18. The method according to claim 15, wherein the control sequence is β-actin.
 19. The method according to claim 18, wherein a target sequence in the β-actin is amplified using a primer comprising the sequence shown in SEQ ID NO: 5 and a primer comprising the sequence shown in SEQ ID NO:
 6. 20. The method according to claim 19, wherein the target sequence is detected using a detectably-labelled probe comprising the sequence shown in SEQ ID NO:
 7. 21. The method according to claim 15, wherein the method is used to assess the extent or to confirm the completeness of enzyme digestion.
 22. A detectably-labelled probe for the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual, which comprises the sequence shown in SEQ ID NO:
 4. 23. A set of primers for the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual, which comprises a primer comprising the sequence shown in SEQ ID NO: 2 and a primer comprising the sequence shown in SEQ ID NO:
 3. 24. A detectably-labelled probe for use as a control during the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual, which comprises the sequence shown in SEQ ID NO:
 7. 25. A set of primers for use as a control during the detection or monitoring of cancer in a biological sample selected from blood, plasma, serum, saliva, urine from an individual, which comprises a primer composing the sequence shown in SEQ ID NO: 5 and a primer comprising the sequence shown in SEQ ID NO:
 6. 